chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14164798	14164799	A	G	82	GENIC	heterozygous	118292398
12	14166749	14166750	T	C	40	GENIC	homozygous	115445268
12	14166756	14166757	T	G	33	GENIC	homozygous	115445270
12	14166760	14166761	G	C	31	GENIC	homozygous	115445272
12	14166761	14166762	G	C	31	GENIC	homozygous	115445274
12	14166773	14166774	C	G	33	GENIC	homozygous	115445277
12	14166786	14166787	T	A	11	GENIC	homozygous	115491735
12	14166788	14166789	G	A	11	GENIC	homozygous	115445279
12	14166792	14166793	A	C	11	GENIC	homozygous	115491737
12	14166796	14166797	T	G	12	GENIC	homozygous	115491739
12	14166806	14166807	T	C	39	GENIC	homozygous	115491741
12	14166807	14166808	T	G	41	GENIC	homozygous	115491743
12	14166823	14166824	G	A	48	GENIC	homozygous	115262335
12	14166824	14166825	G	C	48	GENIC	homozygous	115445281
12	14168355	14168356	C	T	54	GENIC	homozygous	115262337
12	14168629	14168630	T	C	48	GENIC	possibly homozygous	115262339
12	14168932	14168933	C	T	49	GENIC	homozygous	115262341
12	14175276	14175277	C	A	58	GENIC	homozygous	115262347
12	14175737	14175738	A	G	53	GENIC	homozygous	115262349